Skip to main content

Desmethylprodine

ADVERTISEMENT
Identification
Molecular formula
C21H27NO
CAS number
469-99-0
IUPAC name
1,1-diphenyl-4-(1-piperidyl)butan-1-ol
State
State

At room temperature, 1,1-diphenyl-4-(1-piperidyl)butan-1-ol is in a liquid state. It is typically a colorless to pale-yellow liquid with a noticeable chemical odor. The compound boils at high temperatures, greatly surpassing typical room temperature conditions.

Melting point (Celsius)
24.50
Melting point (Kelvin)
297.65
Boiling point (Celsius)
396.20
Boiling point (Kelvin)
669.35
General information
Molecular weight
295.43g/mol
Molar mass
295.4330g/mol
Density
1.1300g/cm3
Appearence

1,1-Diphenyl-4-(1-piperidyl)butan-1-ol is typically found as a colorless to pale-yellow liquid. Its appearance may vary slightly depending on purity and storage conditions. The liquid is noted for its distinct chemical odor.

Comment on solubility

Solubility of 1,1-Diphenyl-4-(1-piperidyl)butan-1-ol

The solubility of 1,1-diphenyl-4-(1-piperidyl)butan-1-ol (C21H27NO) can be quite intriguing due to its complex chemical structure. Understanding its solubility behavior is important for its application in pharmaceutical formulations and organic synthesis. Here are the key points regarding its solubility:

  • Polar versus Nonpolar: This compound features a hydrophobic structural framework due to the presence of multiple phenyl groups, which often limits solubility in polar solvents like water.
  • Solvent Compatibility: It tends to be more soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO), where the nonpolar interactions can be effective.
  • Temperature Dependency: Like many organic compounds, its solubility can increase with temperature, making it beneficial to conduct experiments at higher temperatures to achieve better solute dispersion.
  • Hydrogen Bonding: The alcohol group may allow for some hydrogen bonding interactions, which could enhance solubility in select solvents.

In conclusion, the solubility of 1,1-diphenyl-4-(1-piperidyl)butan-1-ol is influenced by its dual nature as a largely nonpolar molecule that contains a polar functional group. Thus, while it may pose challenges in aqueous environments, suitable organic solvents can facilitate its use across various chemical applications.

Interesting facts

Interesting Facts about 1,1-Diphenyl-4-(1-piperidyl)butan-1-ol

1,1-Diphenyl-4-(1-piperidyl)butan-1-ol is a compound that combines diverse functional groups, making it a subject of interest in various fields such as medicinal chemistry and organic synthesis.

Key Features:

  • Unique Structure: The compound features a butanol backbone with two phenyl rings and a piperidine substituent, leading to its distinctive properties.
  • Pharmacological Relevance: Compounds with similar structures often exhibit interesting pharmacological activities that can potentially be harnessed in drug development.
  • Versatile Synthesis: It can be synthesized through various methods, showcasing the versatility and creativity required in organic chemistry.

Potential Applications:

  • Antidepressants: Research into compounds with piperidine rings has been linked to antidepressant properties, making this compound a candidate for further studies.
  • Anti-anxiety Medications: The structural motifs present could suggest applications in calming or anxiety-reducing medications.
  • Research in Neurochemistry: Due to its potential influence on neurotransmitter systems, it may help in neurochemical studies.

The exploration of 1,1-diphenyl-4-(1-piperidyl)butan-1-ol can lead to the discovery of novel therapeutic agents. As scientists delve into such compounds, they often quote, “Innovation happens at the intersections of different disciplines,” highlighting the importance of interdisciplinary approaches in chemistry.

Synonyms
DIPHENIDOL
Difenidol
972-02-1
Vontrol
Avomol
Nometic
Difenidolo [DCIT]
diphenadol
Difenidolo
Difenidolum
Difenidolum [INN-Latin]
alpha,alpha-Diphenyl-1-piperidinebutanol
1,1-Diphenyl-4-(piperidin-1-yl)butan-1-ol
Diphenyl(3-(1-piperidyl)propyl)carbinol
Diphenidol [USAN]
SKF 478
1,1-diphenyl-4-piperidin-1-ylbutan-1-ol
Difenidol [INN]
SK&F 478
SK&F-478
SK-478
CHEBI:4638
HSDB 3316
EINECS 213-540-9
NQO8R319LY
1-Piperidinebutanol, .alpha.,.alpha.-diphenyl-
BRN 0265884
Benzhydrol, alpha-(3-piperidinopropyl)-
DTXSID3022950
1-Piperidinebutanol, alpha,alpha-diphenyl-
DIPHENIDOL [MI]
DIPHENIDOL [HSDB]
DIPHENIDOL [VANDF]
DIFENIDOL [WHO-DD]
DTXCID502950
SK&F-478A
Difenidol HCl
1-Piperidinebutanol, a,a-diphenyl-
K-478-A
NCGC00016624-03
Difenidolum (INN-Latin)
.alpha.,.alpha.-Diphenyl-1-piperidinebutanol
Normavom
Deiphenidol Hydrochloride
19-11-4
CAS-972-02-1
Diphenidol (USAN/INN)
UNII-NQO8R319LY
Prestwick0_000252
Prestwick1_000252
Prestwick2_000252
Prestwick3_000252
CHEMBL936
SCHEMBL34469
BSPBio_000064
SPBio_002283
BPBio1_000072
GTPL7163
SK&F NO 478-A
OGAKLTJNUQRZJU-UHFFFAOYSA-
1H-INDENE-5-CARBOXYLIC ACID,2,3-DIHYDRO-3-OXO-,ETH
HMS3429M14
HY-A0270
Tox21_113073
BDBM50225701
EX-A10465
AKOS001675735
Tox21_113073_1
AC-4261
DB01231
NCGC00016624-01
NCGC00016624-02
NCGC00016624-05
AS-88604
DA-62864
CAS-3254-89-5
Benzhydrol, .alpha.-(3-piperidinopropyl)-
CS-0017619
NS00040512
1,1-Diphenyl-4-(1-piperidinyl)-1-butanol #
C06961
D03858
EN300-22536348
Q5279734
BRD-K01663662-003-03-8
BRD-K01663662-003-20-2
213-540-9
InChI=1/C21H27NO/c23-21(19-11-4-1-5-12-19,20-13-6-2-7-14-20)15-10-18-22-16-8-3-9-17-22/h1-2,4-7,11-14,23H,3,8-10,15-18H2